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A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis
BACKGROUND: The ability to detect neoplasia-specific fusion genes is important not only in cancer research, but also increasingly in clinical settings to ensure that correct diagnosis is made and the optimal treatment is chosen. However, the available methodologies to detect such fusions all have th...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633275/ https://www.ncbi.nlm.nih.gov/pubmed/19152679 http://dx.doi.org/10.1186/1476-4598-8-5 |
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author | Skotheim, Rolf I Thomassen, Gard OS Eken, Marthe Lind, Guro E Micci, Francesca Ribeiro, Franclim R Cerveira, Nuno Teixeira, Manuel R Heim, Sverre Rognes, Torbjørn Lothe, Ragnhild A |
author_facet | Skotheim, Rolf I Thomassen, Gard OS Eken, Marthe Lind, Guro E Micci, Francesca Ribeiro, Franclim R Cerveira, Nuno Teixeira, Manuel R Heim, Sverre Rognes, Torbjørn Lothe, Ragnhild A |
author_sort | Skotheim, Rolf I |
collection | PubMed |
description | BACKGROUND: The ability to detect neoplasia-specific fusion genes is important not only in cancer research, but also increasingly in clinical settings to ensure that correct diagnosis is made and the optimal treatment is chosen. However, the available methodologies to detect such fusions all have their distinct short-comings. RESULTS: We describe a novel oligonucleotide microarray strategy whereby one can screen for all known oncogenic fusion transcripts in a single experiment. To accomplish this, we combine measurements of chimeric transcript junctions with exon-wise measurements of individual fusion partners. To demonstrate the usefulness of the approach, we designed a DNA microarray containing 68,861 oligonucleotide probes that includes oligos covering all combinations of chimeric exon-exon junctions from 275 pairs of fusion genes, as well as sets of oligos internal to all the exons of the fusion partners. Using this array, proof of principle was demonstrated by detection of known fusion genes (such as TCF3:PBX1, ETV6:RUNX1, and TMPRSS2:ERG) from all six positive controls consisting of leukemia cell lines and prostate cancer biopsies. CONCLUSION: This new method bears promise of an important complement to currently used diagnostic and research tools for the detection of fusion genes in neoplastic diseases. |
format | Text |
id | pubmed-2633275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26332752009-01-31 A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis Skotheim, Rolf I Thomassen, Gard OS Eken, Marthe Lind, Guro E Micci, Francesca Ribeiro, Franclim R Cerveira, Nuno Teixeira, Manuel R Heim, Sverre Rognes, Torbjørn Lothe, Ragnhild A Mol Cancer Research BACKGROUND: The ability to detect neoplasia-specific fusion genes is important not only in cancer research, but also increasingly in clinical settings to ensure that correct diagnosis is made and the optimal treatment is chosen. However, the available methodologies to detect such fusions all have their distinct short-comings. RESULTS: We describe a novel oligonucleotide microarray strategy whereby one can screen for all known oncogenic fusion transcripts in a single experiment. To accomplish this, we combine measurements of chimeric transcript junctions with exon-wise measurements of individual fusion partners. To demonstrate the usefulness of the approach, we designed a DNA microarray containing 68,861 oligonucleotide probes that includes oligos covering all combinations of chimeric exon-exon junctions from 275 pairs of fusion genes, as well as sets of oligos internal to all the exons of the fusion partners. Using this array, proof of principle was demonstrated by detection of known fusion genes (such as TCF3:PBX1, ETV6:RUNX1, and TMPRSS2:ERG) from all six positive controls consisting of leukemia cell lines and prostate cancer biopsies. CONCLUSION: This new method bears promise of an important complement to currently used diagnostic and research tools for the detection of fusion genes in neoplastic diseases. BioMed Central 2009-01-19 /pmc/articles/PMC2633275/ /pubmed/19152679 http://dx.doi.org/10.1186/1476-4598-8-5 Text en Copyright © 2009 Skotheim et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Skotheim, Rolf I Thomassen, Gard OS Eken, Marthe Lind, Guro E Micci, Francesca Ribeiro, Franclim R Cerveira, Nuno Teixeira, Manuel R Heim, Sverre Rognes, Torbjørn Lothe, Ragnhild A A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis |
title | A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis |
title_full | A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis |
title_fullStr | A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis |
title_full_unstemmed | A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis |
title_short | A universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis |
title_sort | universal assay for detection of oncogenic fusion transcripts by oligo microarray analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633275/ https://www.ncbi.nlm.nih.gov/pubmed/19152679 http://dx.doi.org/10.1186/1476-4598-8-5 |
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